Journal
JOURNAL OF THE AMERICAN HEART ASSOCIATION
Volume 1, Issue 4, Pages -Publisher
WILEY
DOI: 10.1161/JAHA.112.001826
Keywords
cholesterol efflux; esterification; reverse cholesterol transport; isotope labeling; stable; sterol excretion
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Funding
- University of California [02-10294]
- Abbott and Merck
- NIH/National Center for Research Resources University of California at San Francisco Clinical and Translational Science Institute [UL1 RR024131]
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Background-Reverse cholesterol transport from peripheral tissues is considered the principal atheroprotective mechanism of high-density lipoprotein, but quantifying reverse cholesterol transport in humans in vivo remains a challenge. We describe here a method for measuring flux of cholesterol though 3 primary components of the reverse cholesterol transport pathway in vivo in humans: tissue free cholesterol (FC) efflux, esterification of FC in plasma, and fecal sterol excretion of plasma-derived FC. Methods and Results-A constant infusion of [ 2,3-C-13(2)]-cholesterol was administered to healthy volunteers. Three-compartment SAAM II (Simulation, Analysis, and Modeling software; SAAM Institute, University of Washington, WA) fits were applied to plasma FC, red blood cell FC, and plasma cholesterol ester C-13-enrichment profiles. Fecal sterol excretion of plasma-derived FC was quantified from fractional recovery of intravenous [ 2,3-C-13(2)]-cholesterol in feces over 7 days. We examined the key assumptions of the method and evaluated the optimal clinical protocol and approach to data analysis and modeling. A total of 17 subjects from 2 study sites (n=12 from first site, age 21 to 75 years, 2 women; n=5 from second site, age 18 to 70 years, 2 women) were studied. Tissue FC efflux was 3.79 +/- 0.88 mg/kg per hour (mean +/- standard deviation), or approximate to 8 g/d. Red blood cell-derived flux into plasma FC was 3.38 +/- 1.10 mg/kg per hour. Esterification of plasma FC was approximate to 28% of tissue FC efflux (1.10 +/- 0.38 mg/kg per hour). Recoveries were 7% and 12% of administered [2,3-C-13(2)]-cholesterol in fecal bile acids and neutral sterols, respectively. Conclusions-Three components of systemic reverse cholesterol transport can be quantified, allowing dissection of this important function of high-density lipoprotein in vivo. Effects of lipoproteins, genetic mutations, lifestyle changes, and drugs on these components can be assessed in humans.
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